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POTASSIUM CHLORIDE

NDC 51662-1387 · HF Acquisition Co LLC, DBA HealthFirst

Generic namePOTASSIUM CHLORIDE
Dosage formINJECTION, SOLUTION, CONCENTRATE
RouteINTRAVENOUS
Active ingredient(s)POTASSIUM CHLORIDE
Strength149 mg/mL
Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
Marketing categoryANDA

Packages

51662-1387-1 — 10 mL in 1 VIAL, SINGLE-DOSE (51662-1387-1)

Billed under HCPCS

J3480 — Injection, potassium chloride, per 2 meq Medicare Part B payment limit (ASP + 6%): $0.14

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7748 — Potassium Chloride, 50090-7749 — Potassium Chloride, 50090-8020 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 50268-671 — Potassium Chloride, 50268-674 — Potassium Chloride, 50268-675 — Potassium Chloride, 51655-226 — Potassium Chloride, 51655-463 — Potassium Chloride, 51655-568 — potassium chloride, 51655-706 — Potassium Chloride, 51662-1421 — POTASSIUM CHLORIDE, 51662-1516 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 51662-1521 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE, 52268-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52268-201 — sodium sulfate, magnesium sulfate, and potassium chloride, 52536-236 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52536-302 — polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride, 53041-420 — Potassium Chloride, 53041-680 — Potassium Chloride, 53041-681 — Potassium Chloride, +445 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.